FDA issued a Warning Letter to Genzyme Corporation on 2/27/2009 as a result of this inspection.
483 Sanofi Genzyme Oct 2008

483 Sanofi Genzyme Oct 2008

Kent Conforti FDA, Debra Emerson FDA, Megan Haggerty FDA$119.00 - Available Now

FDA investigators audited the Sanofi Genzyme - Allston, MA, United States facility and issued inspectional observations (via FDA 483) on 10 Oct 2008.

Product details

  • Category: Human Drugs
  • Inspection end: 10 Oct 2008
  • Location: Allston, United States
  • FEI: 1000305672
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